首页> 外文期刊>Journal of Drug Delivery and Therapeutics >PREPARATION AND EVALUATION OF CARBOXYMETHYL ENSET AND CASSAVA STARCHES AS PHARMACEUTICAL GELLING AGENTS
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PREPARATION AND EVALUATION OF CARBOXYMETHYL ENSET AND CASSAVA STARCHES AS PHARMACEUTICAL GELLING AGENTS

机译:羧甲基淀粉酶和木薯淀粉作为制药胶凝剂的制备与评价

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Starch is usually modified either chemically, physically or enzymatically to augment its convenience for industrial use. In the current study, starches from Enset and cassava plants were carboxymethylated, and factors which affect the carboxymethylation process and degree of substitution (DS) were studied. The application of the carboxymethyl starches as alternative pharmaceutical gelling agents for topical delivery of drugs was also investigated. Accordingly, nine different topical gel formulations of ibuprofen were prepared. All formulations were evaluated with respect to cosmetic qualities, pH, drug content, viscosity, spreadability, extrudability, in vitro drug release, anti-inflammatory activity and stability. The results showed that carboxymethylation was significantly affected by the starch source, reaction medium, temperature and time. All ibuprofen gel formulations showed homogeneous appearance, smooth texture and pleasant odor. The pH values of the formulations ranged from 6.80 to 7.22. Ibuprofen content ranged between 98.76 and 100.20% ensuring the uniformity of the drug content. The cumulative percent ibuprofen released over 12 h across cellulose membrane ranged from 43.8% cm -2 to 84.5% cm -2 . Spreadability, extrudability, the cumulative drug release and diffusion coefficient of ibuprofen were influenced not only by the rheological properties of the formulations but also by the nature of the modified starches. Physicochemically stable ibuprofen gels were obtained with potent anti-inflammatory activities.
机译:淀粉通常经过化学,物理或酶改性,以增加其工业用途的便利性。在当前的研究中,Enset和木薯植物的淀粉被羧甲基化,并且研究了影响羧甲基化过程和取代度(DS)的因素。还研究了羧甲基淀粉作为替代药物胶凝剂在局部给药中的应用。因此,制备了九种不同的布洛芬局部凝胶制剂。对所有制剂进行了化妆品质量,pH,药物含量,粘度,铺展性,可挤出性,体外药物释放,抗炎活性和稳定性方面的评估。结果表明,羧甲基化受到淀粉来源,反应介质,温度和时间的显着影响。所有布洛芬凝胶制剂均表现出均一的外观,光滑的质地和令人愉悦的气味。制剂的pH值在6.80至7.22的范围内。布洛芬含量在98.76至100.20%之间,确保了药物含量的均匀性。布洛芬在12小时内跨纤维素膜释放的累积百分比为43.8%cm -2至84.5%cm -2。布洛芬的延展性,可挤出性,累积药物释放和扩散系数不仅受制剂的流变性质的影响,而且还受到改性淀粉的性质的影响。获得具有强抗炎活性的理化稳定的布洛芬凝胶。

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